Gene Gene information from NCBI Gene database.
Entrez ID 55586
Gene name Myo-inositol oxygenase
Gene symbol MIOX
Synonyms (NCBI Gene)
ALDRL6
Chromosome 22
Chromosome location 22q13.33
miRNA miRNA information provided by mirtarbase database.
132
miRTarBase ID miRNA Experiments Reference
MIRT674440 hsa-miR-483-5p HITS-CLIP 23313552
MIRT691634 hsa-miR-411-5p HITS-CLIP 23313552
MIRT674438 hsa-miR-4781-3p HITS-CLIP 23313552
MIRT674439 hsa-miR-4716-5p HITS-CLIP 23313552
MIRT674436 hsa-miR-4732-3p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0005506 Function Iron ion binding IEA
GO:0005737 Component Cytoplasm IEA
GO:0005737 Component Cytoplasm ISS
GO:0005829 Component Cytosol TAS
GO:0008106 Function Alcohol dehydrogenase (NADP+) activity ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606774 14522 ENSG00000100253
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UGB7
Protein name Inositol oxygenase (EC 1.13.99.1) (Aldehyde reductase-like 6) (Kidney-specific protein 32) (Myo-inositol oxygenase) (MI oxygenase) (Renal-specific oxidoreductase)
PDB 2IBN
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05153 MIOX 37 285 Myo-inositol oxygenase Family
Tissue specificity TISSUE SPECIFICITY: Kidney specific.
Sequence
Sequence length 285
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Ascorbate and aldarate metabolism
Inositol phosphate metabolism
Metabolic pathways
Biosynthesis of nucleotide sugars
  Synthesis of IP2, IP, and Ins in the cytosol
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
HEARING LOSS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
KIDNEY DISEASES CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Renal Cell Renal cell carcinoma Pubtator 37977044 Inhibit
★☆☆☆☆
Found in Text Mining only
Diabetes Diabetes BEFREE 26578517
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes Mellitus BEFREE 26578517
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Diabetes mellitus, type 2 Pubtator 30504713 Stimulate
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Insulin-Dependent Diabetes Mellitus BEFREE 19896870
★☆☆☆☆
Found in Text Mining only
Diabetic Nephropathies Diabetic neuropathy Pubtator 30504713 Associate
★☆☆☆☆
Found in Text Mining only
Diabetic Nephropathy Diabetic Nephropathy BEFREE 28931523, 30504713
★☆☆☆☆
Found in Text Mining only
Fatty Liver Fatty Liver BEFREE 28107998
★☆☆☆☆
Found in Text Mining only
Kidney Failure, Acute Kidney Failure BEFREE 10966922, 24486646, 30581335, 31437128
★☆☆☆☆
Found in Text Mining only
Obesity Obesity BEFREE 26578517
★☆☆☆☆
Found in Text Mining only